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. Author manuscript; available in PMC: 2020 Apr 15.
Published in final edited form as: Biol Psychiatry. 2018 Oct 10;85(8):679–689. doi: 10.1016/j.biopsych.2018.09.030

Figure 6. The primed and IL-1β signature of monocytes recruited to the brain during stress was dependent on IL-6.

Figure 6.

Male WT and IL-6KO C57BL/6 mice were subjected to six repeated cycles of social defeat (Stress) or left undisturbed as controls (n=5). (A) 14 h later, monocytes (CD11b+/CD45hi) in the brain were collected and FAC-sorted. Next, RNA was isolated and mRNA copy number of 279 genes was determined using NanoString gene array. Volcano plot (-log10 (p value) vs. fold change) of genes differentially expressed between brain monocytes from (B) WT stress and WT control groups, (C) IL-6KO stress and WT-stress groups, and (D) IL-6KO stress and IL-6KO control groups. Genes labeled in red (increased) and blue (decreased) were significantly different. (E) Pathways regulated by stress in the wildtype and IL-6KO brain monocytes after stress. (F) Venn diagram depicts genes significantly altered between WT Stress and WT Control but not between IL-6KO Stress and WT Stress (black background), genes significantly altered between WT Stress and WT Control and between IL-6KO Stress and WT Stress (grey background), and genes significantly altered only between the IL-6KO stress and WT stress (p < .05 for all).